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Safety Information
Regulations
This instrument conforms to IEC 60601-1-2:2001.
For U.S.A. and Canada
• When the CX-1 is going to be operated at a voltage of 240V in USA or Canada, be sure to con-
nect the instrument to a center tapped voltage source.
• This instrument is a CLASS I EQUIPMENT according to UL 60601-1 and CAN/CSA C22.2
No. 601.1.
• Grounding reliability can only be achieved when the equipment is connected to an equivalent
receptacle marked “Hospital Only” or “Hospital Grade”.
• The following mark indicates that the instrument is a Type B Applied Parts.
• The degree of protection against ingress of water is IPX0.
• This equipment is not suitable for use in the presence of a flammable anaesthetic mixture with air
or with oxygen or nitrous oxide.
• The mode of operation is Continuous Operation.
For EU Countries
• The following mark shows compliance of the instrument with Directive 93/42/EEC.
• This instrument is a CLASS I EQUIPMENT according to EN 60601-1.
• The following mark indicates that the instrument is a Type B Applied Parts according to EN
60601-1.
• The degree of protection against ingress of water is IPX0.
• This equipment is not suitable for use in the presence of a flammable anaesthetic mixture with air
or with oxygen or nitrous oxide.
• The mode of operation is Continuous Operation.
Für Deutschland
• Während des Betriebs liegt der Schalldruckpegel dieses Instruments bei 70 dB(A) oder weniger
gemäß ISO 7779.
MEDICAL EQUIPMENT WITH RESPECT TO ELECTRICAL SHOCK,
FIRE AND MECHANICAL HAZARDS ONLY
IN ACCORDANCE WITH UL 60601-1 and CAN / CSA C22.2 No. 601.1
41C4